Separation of short and medium‐chain fatty acids using capillary electrophoresis with indirect photometric detection: Part I: Identification of fatty acids in rat feces

Abstract

Short and medium‐chain fatty acids (SMCFAs) are known as essential metabolites found in gut microbiota that function as modulators in the development and progression of many inflammatory conditions as well as in the regulation of cell metabolism. Currently, there are few simple and low‐cost analytical methods available for the determination of SMCFA. This report focuses on SMCFA analysis utilizing CE with indirect photometric detection (CE‐IPD). A ribonucleotide electrolyte, 5’‐adenosine mono‐phosphate (5’‐AMP), is investigated as an IPD reagent due to its high molar absorptivity and dynamic reserve compatible with separation and detection of SMCFA. The operating parameters like the composition of organic solvent, millimolar concentrations of the complexing agent (alpha‐cyclodextrin), 5’‐AMP and non‐absorbing electrolyte (boric acid), as well as the applied voltage, are optimized for resolution, efficiency, and signal‐to‐noise ratio. A baseline resolution of all nine SMCFAs is achieved in less than 15 min. Additionally, the developed CE‐IPD method shows promising potential to identifying SMCFA in rat fecal supernatant. The presented analytical assay is simple, economical, and has considerably good repeatability. The intraday and interday RSD of less than 1 and 2% for relative migration time, as well as less than 14 and 15% for peak area, respectively, were obtained for SMCFA in fecal solution.

Determination of short-chain fatty acids as putative biomarkers of cancer diseases by modern analytical strategies and tools: a review

“…A similar strategy based on CE with indirect UV detection and the use of α-CD as a constituent of the BGE was introduced by Pham et al. ( 184 ) for the determination of SCFAs and medium-chain fatty acids in rat faecal samples. Here, 5’-adenosine mono-phosphate (5’-AMP) was used as an indirect photometric detection reagent.…”

A pre‐column derivatization high‐performance liquid chromatography method for simultaneous determination of short‐chain and medium‐chain fatty acids in a fecal sample

“…Due to the significant impact of SCFAs and MCFAs on biological metabolism, a stable and repeatable method for the quantification of SCFAs and MCFAs in biological samples is particularly essential. The reported method for quantifying SCFAs and MCFAs mainly include CE [21], NMR [22], GC [23], and GC-MS [24]. Because of its high sensitivity and splendid separation ability, GC is widely used in the analysis of FAs.…”